Accès ouvert
2025
article
OpenAlex
Meg K. Tully, Robert J. Commons, J. A. Simpson, David J. Price
In silico pharmacokinetic-pharmacodynamic (PK-PD) models are used to inform dose optimisation in antimalarial drug development. Here the PK-PD models capture the change in parasite count over time because of exposure to antimalarial drug(s). For current deterministic PD models, simulated parasite numbers decline …
au, gb
(code pays fourni par la source)
Accès ouvert
2025
article
OpenAlex
Jing Wang, Seyni Gueye‐Ndiaye, Xiaoyu Li, Sanjana Bhaskar et autres
STUDY OBJECTIVES: To investigate whether gas cooking stove exposure and elevated indoor nitrogen dioxide (NO2) concentration were associated with adverse sleep outcomes in a pediatric sample. METHODS: Children from urban neighborhoods in Boston, Massachusetts underwent in-home sleep assessments. Indoor NO2 concentrations were …
us, cn
(code pays fourni par la source)
Accès ouvert
2025
preprint
OpenAlex
Meg K. Tully, Ruiz Francisco J., J. A. Simpson
In silico pharmacokinetic-pharmacodynamic (PK-PD) models are used to inform dose optimisation in antimalarial drug development. Here the PK-PD models capture the change in parasite count over time due to exposure to antimalarial drug(s). For current deterministic PD models, simulated parasite numbers decline …
au
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Meg K. Tully, S Dini, Jennifer A. Flegg, James McCarthy et autres
The rise of multidrug-resistant malaria requires accelerated development of novel antimalarial drugs. Pharmacokinetic-pharmacodynamic (PK-PD) models relate blood antimalarial drug concentrations with the parasite-time profile to inform dosing regimens. We performed a simulation study to assess the utility of a Bayesian hierarchical mechanistic …
au, gb
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Jing Wang, Seyni Gueye‐Ndiaye, Cecilia Castro‐Diehl, Sanjana Bhaskar et autres
us
(code pays fourni par la source)
Accès ouvert
2024
preprint
OpenAlex
Meg K. Tully, S Dini, Jennifer A. Flegg, James McCarthy et autres
Abstract The rise of multidrug resistant malaria requires accelerated development of novel antimalarial drugs. Pharmacokinetic-pharmacodynamic (PK-PD) models relate blood antimalarial drug concentrations with the parasite-time profile to inform dosing regiments. We performed a simulation study to assess the utility of a Bayesian …
au
(code pays fourni par la source)